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Renee Arbia's Fundraiser:

Turner Syndrome Awareness Month for #VIB Imogen

Renee's Photo
 

Our Butterfly Imogen #VIBImogen
January 31, 2017

Very Important Butterfly, Imogen  See more
Renee Arbia

THE STORY:

Support the Turner Syndrome Global Alliance by donating today for our butterfly Imogen! TSGA was founded by parents of girls and young women with Turner syndrome.(TS) We aim to have a direct impact on the lives of girls, women, and families living with TS by working to include TS in the national conversation on genetic research. We are the voice for a patient and parent perspective as we seek collaboration with scientists, researchers, and doctors to ensure that TS research and resources have meaningful outcomes.

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